Publications

Found 7 results

Filters: Keyword is Humans [Clear All Filters]

2013

Dury AY, Fatimy REl, Tremblay S, Rose TM, Côté J, De Koninck P, Khandjian EW. 2013. Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.. PLoS Genet. 9(10):e1003890.

2012

Flynn R, Labrie-Dion É, Bernier N, Colicos MA, De Koninck P, Zamponi GW. 2012. Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα.. PLoS One. 7(7):e41185.

Fatimy REl, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, Khandjian EW. 2012. Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].. PLoS One. 7(6):e39338.

2006

Davidovic L, Tremblay S, Gravel M, De Koninck P, Khandjian EWMiky. 2006. [The fragile X syndrome: one protein missing and 1001 disoriented mRNAs].. Med Sci (Paris). 22(1):41-6.

Bayer K U, Lebel E, McDonald GL, O'Leary H, Schulman H, De Koninck P. 2006. Transition from reversible to persistent binding of CaMKII to postsynaptic sites and NR2B.. J Neurosci. 26(4):1164-74.

2005

Hudmon A, Lebel E, Roy H, Sik A, Schulman H, M Waxham N, De Koninck P. 2005. A mechanism for Ca2+/calmodulin-dependent protein kinase II clustering at synaptic and nonsynaptic sites based on self-association.. J Neurosci. 25(30):6971-83.

Costantino S, Heinze KG, Martínez OE, De Koninck P, Wiseman PW. 2005. Two-photon fluorescent microlithography for live-cell imaging.. Microsc Res Tech. 68(5):272-6.

Funding

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